Canonical Allele Identifier: PA2827286172
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206227
ClinVar RCV Id: RCV000188256 RCV000764447 RCV000798181 RCV002317130
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317008.1:p.Ala101Gly
CA316103
NM_001330079.2:c.302C>G